- Chapter 1: Structure and Bonding
- Chapter 10: Alkenes
- Chapter 11: Alkynes
- Chapter 12: Oxidation and Reduction
- Chapter 13: Mass Spectrometry and Infrared Spectroscopy
- Chapter 14: Nuclear Magnetic Resonance Spectroscopy
- Chapter 15: Radical Reactions
- Chapter 16: Conjugation, Resonance, and Dienes
- Chapter 17: Benzene and Aromatic Compounds
- Chapter 18: Electrophilic Aromatic Substitution
- Chapter 19: Carboxylic Acids and the Acidity of the OH Bond
- Chapter 2: Acids and Bases
- Chapter 20: Introduction to Carbonyl Chemistry; Organometallic Reagents; Oxidation and Reduction
- Chapter 21: Aldehydes and KetonesNucleophilic Addition
- Chapter 22: Carboxylic Acids and Their DerivativesNucleophilic Acyl Substitution
- Chapter 23: Substitution Reactions of Carbonyl Compounds at the ` Carbon
- Chapter 24: Carbonyl Condensation Reactions
- Chapter 25: Amines
- Chapter 26: CarbonCarbon Bond-Forming Reactions in Organic Synthesis
- Chapter 27: Carbohydrates
- Chapter 28: Amino Acids and Proteins
- Chapter 29: Lipids
- Chapter 3: Introduction to Organic Molecules and Functional Groups
- Chapter 30: Synthetic Polymers
- Chapter 4: Alkanes
- Chapter 5: Stereochemistry
- Chapter 6: Understanding Organic Reactions
- Chapter 7: Alkyl Halides and Nucleophilic Substitution
- Chapter 8: Alkyl Halides and Elimination Reactions
- Chapter 9: Alcohols, Ethers, and Epoxides
Organic Chemistry 3rd Edition - Solutions by Chapter
Full solutions for Organic Chemistry | 3rd Edition
The difference in Gibbs free energy between reactants and a transition state
An OR group.
Benzyl group (C6H5CH2!)
The group derived from toluene by removing a hydrogen from its methyl group.
The experimental measurement of heat produced in chemical and physical processes. (Section 5.5)
A polydentate ligand that is capable of occupying two or more sites in the coordination sphere. (Section 23.3)
The ability to do work.
A biological membrane that consists of a phospholipid bilayer with proteins, carbohydrates, and other lipids on the surface and embedded in the bilayer
A voltaic cell that utilizes the oxidation of a conventional fuel, such as H2 or CH4, in the cell reaction. (Section 20.7)
hexagonal close packing
A crystal structure where the atoms are packed together as closely as possible. The close-packed layers adopt a two-layer repeating pattern, which leads to a primitive hexagonal unit cell. (Section 12.3)
The mixing of different types of atomic orbitals to produce a set of equivalent hybrid orbitals. (Section 9.5)
A nonpolar group that does not have favorable interactions with water.
When signal splitting occurs in 1H NMR spectroscopy, the distance (in hertz) between the individual peaks of a signal.
Experimental conditions under which the composition of the product mixture is determined by the relative rates of formation of each product.
Points in a crystal all of which have identical environments. (Section 12.2)
pressure–volume (PV) work
Work performed by expansion of a gas against a resisting pressure. (Section 5.3)
Secondary structure of nucleic acids
The ordered arrangement of nucleic acid strands
The addition of atoms or groups of atoms to the same face of a carbon-carbon double bond.
A diverse class of naturally occurring compounds that can be thought of as being assembled from isoprene units, each of which contains five carbon atoms.
A compound containing an !SH (sulfhydryl) group bonded to an sp3 -hybridized carbon.
A signal of an NMR spectrum that is shifted toward the right (smaller chemical shift) on the chart paper.